Diaclon Abo/d+ Reverse-group
DiaClon ABO/D+ Reverse-Group blood typing products are being recalled across Canada due to performance issues. This recall affects the product used to determine blood types in medical settings. The recall is classified as Class I, meaning there is a reasonable probability that use of this product could cause serious adverse health consequences or death.
- Product
- DiaClon ABO/D+ Reverse-Group
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-04-09
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9a4d28bc-1bc2-406d-9cc2-e1d2bf31580e